1gr3

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|PDB= 1gr3 |SIZE=350|CAPTION= <scene name='initialview01'>1gr3</scene>, resolution 2.00&Aring;
|PDB= 1gr3 |SIZE=350|CAPTION= <scene name='initialview01'>1gr3</scene>, resolution 2.00&Aring;
|SITE= <scene name='pdbsite=CPS:Cps+Binding+Site+For+Chain+A'>CPS</scene>
|SITE= <scene name='pdbsite=CPS:Cps+Binding+Site+For+Chain+A'>CPS</scene>
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|LIGAND= <scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene> and <scene name='pdbligand=CPS:3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE'>CPS</scene>
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|LIGAND= <scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=CPS:3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE'>CPS</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>
|ACTIVITY=
|ACTIVITY=
|GENE=
|GENE=
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|DOMAIN=
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|RELATEDENTRY=
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1gr3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1gr3 OCA], [http://www.ebi.ac.uk/pdbsum/1gr3 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1gr3 RCSB]</span>
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}}
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==Overview==
==Overview==
Collagen X is expressed specifically in the growth plate of long bones. Its C1q-like C-terminal NC1 domain forms a stable homotrimer and is crucial for collagen X assembly. Mutations in the NC1 domain cause Schmid metaphyseal chondrodysplasia (SMCD). The crystal structure at 2.0 A resolution of the human collagen X NC1 domain reveals an intimate trimeric assembly strengthened by a buried cluster of calcium ions. Three strips of exposed aromatic residues on the surface of NC1 trimer are likely to be involved in the supramolecular assembly of collagen X. Most internal SMCD mutations probably prevent protein folding, whereas mutations of surface residues may affect the collagen X suprastructure in a dominant-negative manner.
Collagen X is expressed specifically in the growth plate of long bones. Its C1q-like C-terminal NC1 domain forms a stable homotrimer and is crucial for collagen X assembly. Mutations in the NC1 domain cause Schmid metaphyseal chondrodysplasia (SMCD). The crystal structure at 2.0 A resolution of the human collagen X NC1 domain reveals an intimate trimeric assembly strengthened by a buried cluster of calcium ions. Three strips of exposed aromatic residues on the surface of NC1 trimer are likely to be involved in the supramolecular assembly of collagen X. Most internal SMCD mutations probably prevent protein folding, whereas mutations of surface residues may affect the collagen X suprastructure in a dominant-negative manner.
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==Disease==
 
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Known diseases associated with this structure: Metaphyseal chondrodysplasia, Schmid type OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120110 120110]], Spondylometaphyseal dysplasia, Japanese type OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120110 120110]]
 
==About this Structure==
==About this Structure==
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[[Category: Singer, J.]]
[[Category: Singer, J.]]
[[Category: Yayon, A.]]
[[Category: Yayon, A.]]
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[[Category: CA]]
 
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[[Category: CPS]]
 
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[[Category: NA]]
 
[[Category: collagen]]
[[Category: collagen]]
[[Category: connective tissue]]
[[Category: connective tissue]]
[[Category: extracellular matrix]]
[[Category: extracellular matrix]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 11:26:55 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 20:49:39 2008''

Revision as of 17:49, 30 March 2008


PDB ID 1gr3

Drag the structure with the mouse to rotate
, resolution 2.00Å
Sites:
Ligands: , ,
Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



STRUCTURE OF THE HUMAN COLLAGEN X NC1 TRIMER


Overview

Collagen X is expressed specifically in the growth plate of long bones. Its C1q-like C-terminal NC1 domain forms a stable homotrimer and is crucial for collagen X assembly. Mutations in the NC1 domain cause Schmid metaphyseal chondrodysplasia (SMCD). The crystal structure at 2.0 A resolution of the human collagen X NC1 domain reveals an intimate trimeric assembly strengthened by a buried cluster of calcium ions. Three strips of exposed aromatic residues on the surface of NC1 trimer are likely to be involved in the supramolecular assembly of collagen X. Most internal SMCD mutations probably prevent protein folding, whereas mutations of surface residues may affect the collagen X suprastructure in a dominant-negative manner.

About this Structure

1GR3 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Insight into Schmid metaphyseal chondrodysplasia from the crystal structure of the collagen X NC1 domain trimer., Bogin O, Kvansakul M, Rom E, Singer J, Yayon A, Hohenester E, Structure. 2002 Feb;10(2):165-73. PMID:11839302

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